EP1852438B1 - Tantalverbindung, verfahren zu deren herstellung, tantalhaltiger dünner film und verfahren zu dessen herstellung - Google Patents
Tantalverbindung, verfahren zu deren herstellung, tantalhaltiger dünner film und verfahren zu dessen herstellung Download PDFInfo
- Publication number
- EP1852438B1 EP1852438B1 EP06712311A EP06712311A EP1852438B1 EP 1852438 B1 EP1852438 B1 EP 1852438B1 EP 06712311 A EP06712311 A EP 06712311A EP 06712311 A EP06712311 A EP 06712311A EP 1852438 B1 EP1852438 B1 EP 1852438B1
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- EP
- European Patent Office
- Prior art keywords
- tantalum
- thin film
- group
- general formula
- containing thin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 229910052715 tantalum Inorganic materials 0.000 title claims abstract description 69
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 title claims abstract description 61
- 238000000034 method Methods 0.000 title claims abstract description 53
- 150000003482 tantalum compounds Chemical class 0.000 title claims abstract description 44
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 8
- 239000010409 thin film Substances 0.000 title claims description 67
- 239000002994 raw material Substances 0.000 claims abstract description 37
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 15
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 11
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 17
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 11
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 9
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 9
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims description 3
- 125000004665 trialkylsilyl group Chemical group 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 abstract description 8
- 150000002367 halogens Chemical class 0.000 abstract description 8
- 239000000126 substance Substances 0.000 abstract 3
- 239000010408 film Substances 0.000 description 36
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
- 239000007789 gas Substances 0.000 description 27
- -1 amide compound Chemical class 0.000 description 26
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 24
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 24
- 230000015572 biosynthetic process Effects 0.000 description 22
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 20
- 239000007787 solid Substances 0.000 description 20
- 238000005229 chemical vapour deposition Methods 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- 238000000231 atomic layer deposition Methods 0.000 description 16
- 239000002904 solvent Substances 0.000 description 16
- 239000000758 substrate Substances 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 15
- 238000004833 X-ray photoelectron spectroscopy Methods 0.000 description 12
- 229910052786 argon Inorganic materials 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- LYODYUYNBMSJCS-UHFFFAOYSA-N C(C)C1(C=CC=C1)[Ta](C=O)C1(C=CC=C1)CC Chemical compound C(C)C1(C=CC=C1)[Ta](C=O)C1(C=CC=C1)CC LYODYUYNBMSJCS-UHFFFAOYSA-N 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 10
- UHOVQNZJYSORNB-MZWXYZOWSA-N benzene-d6 Chemical compound [2H]C1=C([2H])C([2H])=C([2H])C([2H])=C1[2H] UHOVQNZJYSORNB-MZWXYZOWSA-N 0.000 description 10
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical class C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 10
- 229910052710 silicon Inorganic materials 0.000 description 10
- 239000010703 silicon Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 description 10
- OEIMLTQPLAGXMX-UHFFFAOYSA-I tantalum(v) chloride Chemical compound Cl[Ta](Cl)(Cl)(Cl)Cl OEIMLTQPLAGXMX-UHFFFAOYSA-I 0.000 description 10
- 239000012159 carrier gas Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 229910004537 TaCl5 Inorganic materials 0.000 description 7
- 229910052802 copper Inorganic materials 0.000 description 7
- 239000010949 copper Substances 0.000 description 7
- 229910052814 silicon oxide Inorganic materials 0.000 description 7
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 6
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 6
- 239000003638 chemical reducing agent Substances 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 5
- 238000005160 1H NMR spectroscopy Methods 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- 239000000706 filtrate Substances 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 238000001308 synthesis method Methods 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 238000002076 thermal analysis method Methods 0.000 description 5
- 239000008096 xylene Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- LVKCSZQWLOVUGB-UHFFFAOYSA-M magnesium;propane;bromide Chemical compound [Mg+2].[Br-].C[CH-]C LVKCSZQWLOVUGB-UHFFFAOYSA-M 0.000 description 4
- 238000001819 mass spectrum Methods 0.000 description 4
- 238000000682 scanning probe acoustic microscopy Methods 0.000 description 4
- 239000006228 supernatant Substances 0.000 description 4
- BITWLJPZLYJJGM-UHFFFAOYSA-N C(C)C1(C=CC=C1)[TaH3]C1(C=CC=C1)CC Chemical compound C(C)C1(C=CC=C1)[TaH3]C1(C=CC=C1)CC BITWLJPZLYJJGM-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 238000005240 physical vapour deposition Methods 0.000 description 3
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- 239000012279 sodium borohydride Substances 0.000 description 3
- 229910000033 sodium borohydride Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IQSUNBLELDRPEY-UHFFFAOYSA-N 1-ethylcyclopenta-1,3-diene Chemical compound CCC1=CC=CC1 IQSUNBLELDRPEY-UHFFFAOYSA-N 0.000 description 2
- SHJSSPHUBNWEDZ-UHFFFAOYSA-N C(CC)C1(C=CC=C1)C(=O)[Ta] Chemical compound C(CC)C1(C=CC=C1)C(=O)[Ta] SHJSSPHUBNWEDZ-UHFFFAOYSA-N 0.000 description 2
- JEDZLBFUGJTJGQ-UHFFFAOYSA-N [Na].COCCO[AlH]OCCOC Chemical compound [Na].COCCO[AlH]OCCOC JEDZLBFUGJTJGQ-UHFFFAOYSA-N 0.000 description 2
- OPICPBLVZCCONG-UHFFFAOYSA-N [Ta].[C]=O Chemical compound [Ta].[C]=O OPICPBLVZCCONG-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- FPNFSSWCUULLCP-UHFFFAOYSA-N carbanide;tantalum(5+) Chemical compound [CH3-].[CH3-].[CH3-].[CH3-].[CH3-].[Ta+5] FPNFSSWCUULLCP-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 150000001793 charged compounds Chemical class 0.000 description 2
- 239000007810 chemical reaction solvent Substances 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 239000004210 ether based solvent Substances 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- ZBDWUWNQBVXRMA-UHFFFAOYSA-N lithium;5-ethylcyclopenta-1,3-diene Chemical compound [Li+].CC[C-]1C=CC=C1 ZBDWUWNQBVXRMA-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- OSFBJERFMQCEQY-UHFFFAOYSA-N propylidene Chemical compound [CH]CC OSFBJERFMQCEQY-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000012419 sodium bis(2-methoxyethoxy)aluminum hydride Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- GCPVYIPZZUPXPB-UHFFFAOYSA-I tantalum(v) bromide Chemical compound Br[Ta](Br)(Br)(Br)Br GCPVYIPZZUPXPB-UHFFFAOYSA-I 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 230000008016 vaporization Effects 0.000 description 2
- IFZHGQSUNAKKSN-UHFFFAOYSA-N 1,1-diethylhydrazine Chemical compound CCN(N)CC IFZHGQSUNAKKSN-UHFFFAOYSA-N 0.000 description 1
- DIIIISSCIXVANO-UHFFFAOYSA-N 1,2-Dimethylhydrazine Chemical compound CNNC DIIIISSCIXVANO-UHFFFAOYSA-N 0.000 description 1
- QZOJRSAENHTURL-UHFFFAOYSA-N 1-azidobutane Chemical compound CCCCN=[N+]=[N-] QZOJRSAENHTURL-UHFFFAOYSA-N 0.000 description 1
- RZPAXISDLOEXPI-UHFFFAOYSA-N 1-propylcyclopenta-1,3-diene Chemical compound CCCC1=CC=CC1 RZPAXISDLOEXPI-UHFFFAOYSA-N 0.000 description 1
- UHCHTNNVHZPRBF-UHFFFAOYSA-N C1(C=CC=C1)[TaH3]C1C=CC=C1 Chemical compound C1(C=CC=C1)[TaH3]C1C=CC=C1 UHCHTNNVHZPRBF-UHFFFAOYSA-N 0.000 description 1
- OSHGSBOTPMAEAF-UHFFFAOYSA-L Cl[Ta](C1(C=CC=C1)CCC)(C1(C=CC=C1)CCC)Cl Chemical compound Cl[Ta](C1(C=CC=C1)CCC)(C1(C=CC=C1)CCC)Cl OSHGSBOTPMAEAF-UHFFFAOYSA-L 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910010084 LiAlH4 Inorganic materials 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229910007161 Si(CH3)3 Inorganic materials 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- XKLVLDXNZDIDKQ-UHFFFAOYSA-N butylhydrazine Chemical compound CCCCNN XKLVLDXNZDIDKQ-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- MROCJMGDEKINLD-UHFFFAOYSA-N dichlorosilane Chemical compound Cl[SiH2]Cl MROCJMGDEKINLD-UHFFFAOYSA-N 0.000 description 1
- VSLPMIMVDUOYFW-UHFFFAOYSA-N dimethylazanide;tantalum(5+) Chemical compound [Ta+5].C[N-]C.C[N-]C.C[N-]C.C[N-]C.C[N-]C VSLPMIMVDUOYFW-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- PZPGRFITIJYNEJ-UHFFFAOYSA-N disilane Chemical compound [SiH3][SiH3] PZPGRFITIJYNEJ-UHFFFAOYSA-N 0.000 description 1
- UCSVJZQSZZAKLD-UHFFFAOYSA-N ethyl azide Chemical compound CCN=[N+]=[N-] UCSVJZQSZZAKLD-UHFFFAOYSA-N 0.000 description 1
- WHRIKZCFRVTHJH-UHFFFAOYSA-N ethylhydrazine Chemical compound CCNN WHRIKZCFRVTHJH-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- NFFIWVVINABMKP-UHFFFAOYSA-N methylidynetantalum Chemical compound [Ta]#C NFFIWVVINABMKP-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- HDZGCSFEDULWCS-UHFFFAOYSA-N monomethylhydrazine Chemical compound CNN HDZGCSFEDULWCS-UHFFFAOYSA-N 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- BPUBBGLMJRNUCC-UHFFFAOYSA-N oxygen(2-);tantalum(5+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ta+5].[Ta+5] BPUBBGLMJRNUCC-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-BJUDXGSMSA-N oxygen-15 atom Chemical compound [15O] QVGXLLKOCUKJST-BJUDXGSMSA-N 0.000 description 1
- QVGXLLKOCUKJST-NJFSPNSNSA-N oxygen-18 atom Chemical compound [18O] QVGXLLKOCUKJST-NJFSPNSNSA-N 0.000 description 1
- QVGXLLKOCUKJST-AKLPVKDBSA-N oxygen-19 atom Chemical compound [19O] QVGXLLKOCUKJST-AKLPVKDBSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000005003 perfluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- 125000005004 perfluoroethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 125000005005 perfluorohexyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- 125000005008 perfluoropentyl group Chemical group FC(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)* 0.000 description 1
- 125000005009 perfluoropropyl group Chemical group FC(C(C(F)(F)F)(F)F)(F)* 0.000 description 1
- CTRLRINCMYICJO-UHFFFAOYSA-N phenyl azide Chemical compound [N-]=[N+]=NC1=CC=CC=C1 CTRLRINCMYICJO-UHFFFAOYSA-N 0.000 description 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- 229940067157 phenylhydrazine Drugs 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000008054 signal transmission Effects 0.000 description 1
- 229910021332 silicide Inorganic materials 0.000 description 1
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 description 1
- FDNAPBUWERUEDA-UHFFFAOYSA-N silicon tetrachloride Chemical compound Cl[Si](Cl)(Cl)Cl FDNAPBUWERUEDA-UHFFFAOYSA-N 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 238000005092 sublimation method Methods 0.000 description 1
- 229910003468 tantalcarbide Inorganic materials 0.000 description 1
- 229910001936 tantalum oxide Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000002230 thermal chemical vapour deposition Methods 0.000 description 1
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 description 1
- 239000005052 trichlorosilane Substances 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 239000006200 vaporizer Substances 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/06—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of metallic material
- C23C16/18—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of metallic material from metallo-organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F19/00—Metal compounds according to more than one of main groups C07F1/00 - C07F17/00
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/34—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies not provided for in groups H01L21/0405, H01L21/0445, H01L21/06, H01L21/16 and H01L21/18 with or without impurities, e.g. doping materials
- H01L21/44—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/38 - H01L21/428
Definitions
- the present invention relates to a novel tantalum compound and a method for producing the same.
- the tantalum compound of the present invention is useful for the formation of a tantalum-containing thin film by a chemical vapor deposition method (CVD method) or an atomic layer deposition method (ALD method). Further, it relates to a method for forming a tantalum-containing thin film which is useful for the production of semiconductor devices.
- CVD method chemical vapor deposition method
- ALD method atomic layer deposition method
- the tantalum nitride film has poor adhesion to a copper seed film for forming a copper wiring by plating, and film peeling occurs between the tantalum nitride film and the copper seed film when forming a wiring or planarizing after wiring formation, resulting in generation of defect.
- a method is employed that a metallic tantalum film is formed between the tantalum nitride film as a barrier film and the copper seed film, thereby preventing the film peeling.
- a tantalum nitride film and a metallic tantalum film are mainly formed by a physical vapor deposition method (PVD method) by sputtering.
- PVD method physical vapor deposition method
- CVD method chemical vapor deposition method
- ALD method atomic layer deposition method
- a tantalum nitride film or a metallic tantalum film is formed by CVD method or ALD method, it is desirable that both films can be formed from the same tantalum raw material in one reaction chamber.
- a halide such as TaCl 5 and TaBr 5 is investigated (for example, see Non-Patent Document 1).
- the halide has high melting point and is required to vaporize by sublimation. Thus, it is difficult to use the halide as a raw material in CVD method or ALD method. Additionally, there are the problems on corrosion of a film due to a residual halogen in a film, deterioration of adhesion and the like. On the other hand, in the amide compound, because nitrogen remains in a film, it is possible to form a tantalum nitride film, but it is difficult to form a metallic tantalum film.
- a tantalum raw material for CVD or ALD that does not contain a halogen and nitrogen in the molecule is required, and a method of using an organometallic compound such as ((Si(CH 3 ) 3 )C 5 H 4 )Ta(CO) (see Patent Document 1) or ((Si (CH 3 ) 3 )C 5 H 4 ) 2 TaH 3 (see Patent Document 2) is investigated.
- an organometallic compound such as ((Si(CH 3 ) 3 )C 5 H 4 )Ta(CO) (see Patent Document 1) or ((Si (CH 3 ) 3 )C 5 H 4 ) 2 TaH 3 (see Patent Document 2) is investigated.
- an organometallic compound such as ((Si(CH 3 ) 3 )C 5 H 4 )Ta(CO) (see Patent Document 1) or ((Si (CH 3 ) 3 )C 5 H 4 ) 2 TaH 3 (see Patent Document 2) is investigated.
- an organometallic compound such as ((
- Cp 2 TaH 3 (see Non-Patent Document 4) and Cp 2 Ta(CO)H (see Non-Patent Document 5) are known a tantalum-containing organometallic compound.
- US-A-5 130 172 discloses a process for forming, a tantalum-containing thin film which comprises using pentamethyltantalum, i.e. Ta(CH 3 ) 5 or bis(cyclo pentadienyl)trihydridotantalum, i.e. (cp) 2 TaH 3 , as a raw material.
- pentamethyltantalum i.e. Ta(CH 3 ) 5
- bis(cyclo pentadienyl)trihydridotantalum i.e. (cp) 2 TaH 3
- WO 2004/065650 A2 discloses chemical vapor deposition precursors for deposition of tantalum-based materials.
- a first object of the present invention is to provide a novel tantalum compound which does not contain a halogen and nitrogen in its molecule, and enables to selectively form a tantalum-containing thin film which does not contain those elements, and various tantalum-containing thin films containing the desired element by the addition of a reactive gas, and a method for producing the same. Further, a second object of the present invention is to provide a method for stably forming a tantalum-containing thin film which contains the desired element, and a tantalum-containing thin film which contains an optional element.
- tantalum compounds represented by the following general formula (1).
- the first invention is a tantalum compound characterized in that it is represented by the following general formula (1) in which R 1 represents an ethyl group or a propyl group.
- the tantalum compound represented by the general formula (1) which is characterized by reacting carbon monoxide with a tantalum compound represented by the following general formula (2) in which R 2 represents an ethyl group or a propyl group.
- the present inventors have found that the above second object can be achieved by using a tantalum compound represented by the following general formula (6) as a raw material.
- a novel tantalum compound of the present invention can be used as a raw material of a tantalum-containing thin film by CVD method or ALD method from its vaporization and decomposition characteristics. Further, because of not containing a halogen and nitrogen in its molecule, it is possible to form a tantalum-containing thin film which does not contain those elements, and to form various tantalum-containing thin films which contain the desired element by the addition of a reactive gas. Further, a novel tantalum compound of the present invention can expect a function as a reaction catalyst.
- the method for forming a tantalum-containing thin film of the present invention makes it possible to stably form various tantalum thin films containing the desired element, such as a metallic tantalum thin film and a tantalum nitride thin film.
- Cp means a cyclopentadienyl group
- Et means an ethyl group
- Pr means a propyl group
- Bu means a butyl group
- THF means tetrahydrofuran
- the tantalum compound represented by the above general formula (2) which does not form part of the invention, can be synthesized by using a tantalum halide such as TaCl 5 shown by the general formula (3) as a raw material.
- the synthesis method can apply a method known as the synthesis method of TaCp 2 H 3 .
- the following method can be applied; a method of reacting the tantalum halide represented by the above general formula (3) and isopropyl magnesium bromide, reacting an alkali metal salt of the substituted cyclopentadiene represented by the general formula (4) to synthesize a tantalum compound represented by the general formula (5) in which R 2 represents an ethyl group or a propyl, and X represents a halogen, and reacting a reducing agent with this compound to synthesize, as described in M. L. H. Green and B. Jousseaume, J. Organomet. Chem.
- TaCl 5 , TaBr 5 , TaI 5 and the like can be used, and TaCl 5 is preferable in the points of cost and availability.
- the reducing agent NaAlH 2 (OCH 2 CH 2 OCH 3 ) 2 , NaBH 4 , LiAlH 4 and the like can be used.
- the alkali metal salt of the substituted cyclopentadiene is preferably Na salts, K salts and Li salts.
- ether solvents such as diethyl ether and THF
- hydrocarbon solvents such as hexane, heptane, octane, toluene and xylene can be used.
- the tantalum compound represented by the above general formula (1) can be synthesized by reacting carbon monoxide with the tantalum compound represented by the general formula (2).
- the reaction can be conducted in a carbon monoxide atmosphere under pressure or at normal pressures by dissolving or suspending the tantalum compound represented by the general formula (2) in a solvent.
- a solvent used is preferably a hydrocarbon solvent having a boiling point of 100°C or higher, such as toluene, xylene, octane, nonane and decane.
- the substituent R 2 in the tantalum compound represented by the general formula (2) directly constitutes the substituent R 1 in the tantalum compound represented by the general formula (1) without receiving change by this reaction.
- the tantalum compound represented by the above general formula (1) can be vaporized at 200°C or lower from thermal analysis (TG and DSC) and thermally decompose at 200 to 300°C. Therefore, this compound can be used as a raw material for the formation of a tantalum-containing thin film by CVD method or ALD method.
- a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, an isopropyl group, a tert-butyl group and the like can be exemplified as the alkyl group having from 1 to 6 carbon atoms, and a trimethylsilyl group, an ethyldimethylsilyl group, a diethylmethylsilyl group, a triethylsilyl group and the like can be exemplified as the trialkylsilyl group having from 3 to 6 carbon atoms shown by R 3 , R 4 , R 5 and R 6 .
- a trifluoromethyl group, a perfluoroethyl group, a perfluoropropyl group, a perfluorobutyl group, a perfluoropentyl group, a perfluorohexyl group, a perfluoroisopropyl group, a perfluoro-tert-butyl group and the like can be exemplified as the alkyl group having from 1 to 6 carbon atoms which may be substituted with at least one fluorine atom.
- the second invention is characterized in that the tantalum compound of the above general formula (6) is used as a raw material of a tantalum-containing thin film, but a method for forming the tantalum-containing thin film from the tantalum compound of the above general formula (6) is not particularly limited.
- CVD method or ALD method is preferable as a film-forming method.
- a raw material preferably has low melting point and high vapor pressure.
- R 4 and R 6 are a hydrogen atom
- R 3 and R 5 are a straight-chain alkyl group having from 1 to 4 carbon atoms, a trimethylsilyl group or a trifluoromethyl group
- R 4 and R 6 are a hydrogen atom
- R 3 and R 5 are a straight-chain alkyl group having from 2 to 4 carbon atoms.
- R 4 and R 6 are a hydrogen atom, and R 3 and R 5 are an ethyl group or a propyl group, and it is particularly preferable that R 4 and R 6 are a hydrogen atom, and R 3 and R 5 are an ethyl group.
- the tantalum compound represented by the above general formula (6) can be synthesized by reacting carbon monoxide with Ta((R 3 ) j (R 4 ) k Cp)((R 5 ) m (R 6 ) n Cp)H 3 that can be synthesized from a tantalum halide such as TaCl 5 .
- the synthesis method of Ta((R 3 ) j (R 4 ) k Cp)((R 5 ) m (R 6 ) n Cp)H 3 can apply a method known as the synthesis method of TaCp 2 H 3 when (R 3 ) j (R 4 ) k Cp and (R 5 ) m (R 6 ) n Cp are the same.
- the following method can be applied; a synthesis method by reacting a tantalum halide and isopropyl magnesium bromide, reacting an alkali metal salt of a substituted cyclopendadiene to synthesize Ta((R 3 ) j (R 4 ) k Cp)((R 5 ) m (R 6 ) n Cp)X 2 (X represents a halogen), and reacting a reducing agent with this, as described in M. L. H. Green and B. Jousseaume, J. Organomet. Chem.
- TaCl 5 As the tantalum halide, TaCl 5 , TaBrs, TaI 5 and the like can be used, and TaCl 5 is preferable from the points of cost and availability.
- the reducing agent NaAlH 2 (OCH 2 CH 2 OCH 3 ) 2 , NaBH 4 , LiAlB 4 and the like can be used.
- the alkali metal salt of the substituted cyclopentadiene is preferably Na salts, K salts and Li salts.
- ether solvents such as diethyl ether and THF
- hydrocarbon solvents such as hexane, heptane, octane, toluene and xylene can be used.
- the reaction of Ta ((R 3 ) j (R 4 ) k Cp) ((R 5 ) m (R 6 ) n Cp) H 3 and carbon monoxide can be conducted in a state of dissolving or dispersing in a solvent under pressure or at normal pressures in a carbon monoxide atmosphere.
- a solvent used is preferably a hydrocarbon solvent having a boiling point of 100°C or higher, such as toluene, xylene, octane, nonane and decane.
- the tantalum compound represented by the general formula (6) is not particularly limited so far as it does not react with the tantalum compound, and hydrocarbon solvents such as hexane, cyclohexane, heptane, octane, toluene and xylene are preferably used.
- a raw material is gasified and supplied onto a substrate, and its method can be carried out by a bubbling method of blowing a carrier gas such as Ar into a liquefied raw material and supplying the raw material gas together with the carrier gas onto a substrate; a sublimation method of heating a solid raw material to sublimate and supplying the raw material gas together with a carrier gas onto a substrate; a liquid injection method of vaporizing a liquefied raw material or a solution of a raw material in a vaporizer and supplying the gas onto a substrate; and the like.
- a bubbling method of blowing a carrier gas such as Ar into a liquefied raw material and supplying the raw material gas together with the carrier gas onto a substrate
- a sublimation method of heating a solid raw material to sublimate and supplying the raw material gas together with a carrier gas onto a substrate
- a liquid injection method of vaporizing a liquefied raw material or a solution of a raw material in a
- Formation of a thin film is carried out by decomposing a raw material supplied onto a substrate. It is possible to conduct the decomposition with only heat, but plasma, light and the like may be used together. In forming the thin film, it is possible to change the composition of the thin film by coexisting a reactive gas.
- a metallic tantalum thin film by supplying a reducing gas such as hydrogen, followed by film formation, and it is possible to form a tantalum nitride thin film by supplying a N-containing gas such as ammonia, methylhydrazine, dimethylhydrazine, ethylhydrazine, diethylhydrazine, butylhydrazine, phenylhydrazine, ethyl azide, butyl azide or phenyl azide, followed by film formation.
- a reducing gas such as hydrogen
- tantalum silicide thin film by supplying a Si-containing gas such as monosilane, disilane, dichlorosilane, trichlorosilane or tetrachlorosilane, followed by film formation, and it is possible to form a tantalum oxide thin film by supplying an oxygen-containing gas such as oxygen, ozone or water vapor, followed by film formation. It is further possible to form a tantalum carbide thin film, a tantalum carbonitride thin film and a tantalum siliconitride thin film, depending on the combination of reactive gases, film formation conditions and the like.
- Si-containing gas such as monosilane, disilane, dichlorosilane, trichlorosilane or tetrachlorosilane
- Film-forming methods other than CVD method and ALD method for example, film-forming methods by a spin coating method, a dipping method, a spraying method and the like that supply a raw material in a form of a liquid or a solution, are included in the present invention.
- the tantalum compound obtained has a wide temperature range at which the compound can vaporize stably without decomposition, and thermally decomposes in the vicinity of 260°C, and the compound is therefore suitable as a raw material of a tantalum-containing thin film by CVD method or ALD method
- 1 H-NMR Benzene-d 6 , ⁇ ppm
- 4.52 m, 4H, C 5 H 4 Br
- 4.46 m, 2H, C 5 H 4 Pr
- 4.41 m, 2H, C 5 H 4 Br
- a cylinder containing hydridobis (propylcyclopentadienyl)carbonyltantalum therein was heated to 100°C, inner pressure was maintained at 13.33 kPa (100 Torr), and an argon gas as a carrier gas was blown at a flow rate of 100 seem to vaporize the compound.
- This was diluted with an argon gas at a flow rate of 100 sccm, and introduced into a reaction chamber maintained at 0.53 kPa (4 Torr).
- This gas was thermally decomposed on a silicon oxide/silicon substrate heated to 400°C to deposit a thin film thereon.
- XPS X-ray photoelectron spectroscopy analyzer
- a cylinder containing hydridobis(propylcyolopentadienyl)carbonyltantalum therein was heated to 100°C, inner pressure was maintained at 13.33 kPa (100 Torr), and an argon gas as a carrier gas was blown at a flow rate of 100 sccm to vaporize the compound.
- This was diluted with an argon gas at a flow rate of 100 sccm, and introduced into a reaction chamber maintained at 0.53 kPa (4 Torr), and at the same time, an ammonia gas was introduced into the reaction chamber at a flow rate of 2 sccm.
- This gas was thermally decomposed on a silicon oxide/silicon substrate heated to 400°C to deposit a thin film thereon.
- XPS X-ray photoelectron spectroscopy analyzer
- tantalum-containing thin film on silicon oxide/silicon substrate by thermal CVD method using bis(ethylcyclopentadienyl)hydridocarbonyltantalum as raw material
- a cylinder containing bis(ethylcyclopentadienyl)-hydridocarbonyltantalum therein was heated to 90°C, inner pressure was maintained at 13.33 kPa (100 Torr), and an argon gas as a carrier gas was blown at a flow rate of 100 sccm to vaporize the compound. This was diluted with an argon gas at a flow rate of 100 sccm, and introduced into a reaction chamber maintained at 1.33 kPa (10 Torr). This gas was thermally decomposed on a silicon oxide/silicon substrate heated to 600°C to deposit a thin film thereon.
- XPS X-ray photoelectron spectroscopy analyzer
- a cylinder containing bis(ethylcyclopentadienyl)-hydridocarbonyltantalum therein was heated to 90°C, inner pressure was maintained at 6.67 kPa (50 Torr), and an argon gas as a carrier gas was blown at a flow rate of 28 sccm to vaporize the compound.
- This was introduced into a plasma-generating reaction chamber maintained at 0.2 kPa (1.5 ⁇ 10 -3 Torr) to deposit a thin film on a silicon oxide/silicon substrate heated to 300°C.
- Plasma was generated by 2.45 GHz, 600W microwave and 875G applied magnetic field in an argon gas at a flow rate of 10 sccm.
- XPS X-ray photoelectron spectroscopy analyzer
- a cylinder containing bis(ethylcyclopentadienyl)-hydridocarbonyltantalum therein was heated to 90°C, inner pressure was maintained at 6.67 kPa (50 Torr), and an argon gas as a carrier gas was blown at a flow rate of 28 sccm to vaporize the compound.
- This was introduced into a plasma-generating reaction chamber maintained at 0.2 kPa (1.5 ⁇ 10 -3 Torr) to deposit a thin film on a silicon substrate heated to 400°C.
- Plasma was generated by 2.45 GHz, 600W microwave and 875G applied magnetic field in an argon gas at a flow rate of 10 sccm.
- XPS X-ray photoelectron spectroscopy analyzer
- a cylinder containing bis(ethylcyclopentadienyl)-hydridocarbonyltantalum therein was heated to 90°C, inner pressure was maintained at 9.33 kPa (70 Torr), and an argon gas as a carrier gas was blown at a flow rate of 55 sccm to vaporize the compound.
- This was introduced into a plasma-generating reaction chamber maintained at 1 Pa (7.5 ⁇ 10 -3 Torr) to deposit a thin film on a silicon substrate heated to 300°C.
- Plasma was generated by 2.45 GHz, 600W microwave and 875G applied magnetic field in an argon gas containing 4% hydrogen at a flow rate of 40 sccm.
- a novel tantalum compound which enables to selectively form a tantalum-containing thin film free of halogen and the like, and various tantalum-containing thin films which contain the desired element, and a method for producing the same can be provided. Further, a method for stably forming a tantalum-containing thin film which contains the desired element can be provided.
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Claims (7)
- Tantalverbindung nach Anspruch 1, dadurch gekennzeichnet, dass R1 eine Ethylgruppe ist.
- Verfahren zur Herstellung einer Tantalverbindung, die durch die folgende allgemeine Formel (1) dargestellt ist:
das das Zur-Reaktion-Bringen von Kohlenmonoxid mit einer Tantalverbindung umfasst, die durch die folgende allgemeine Formel (2) dargestellt ist: - Verfahren zur Herstellung einer tantalhaltigen Dünnschicht, das die Verwendung einer Tantalverbindung als einen Ausgangsstoff umfasst, die durch die folgende allgemeine Formel (6) dargestellt ist:
- Verfahren zur Herstellung einer tantalhaltigen Dünnschicht nach Anspruch 4, dadurch gekennzeichnet, dass j = 1 ist, m = 1 ist, R3 und R5 eine geradkettige Alkylgruppe mit 2 bis 4 Kohlenstoffatomen sind und R4 und R6 ein Wasserstoffatom sind.
- Verfahren zur Herstellung einer tantalhaltigen Dünnschicht nach Anspruch 5, dadurch gekennzeichnet, dass j = 1 ist, m = 1 ist, R3 und R5 eine Ethylgruppe oder eine Propylgruppe sind und R4 und R6 ein Wasserstoffatom sind.
- Verfahren zur Herstellung einer tantalhaltigen Dünnschicht nach Anspruch 6, dadurch gekennzeichnet, dass j = 1 ist, m = 1 ist, R3 und R5 eine Ethylgruppe sind und R4 und R6 ein Wasserstoffatom sind.
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JP2005243053 | 2005-08-24 | ||
PCT/JP2006/301116 WO2006082739A1 (ja) | 2005-02-02 | 2006-01-25 | タンタル化合物、その製造方法、タンタル含有薄膜、及びその形成方法 |
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EP (1) | EP1852438B1 (de) |
JP (1) | JP5053543B2 (de) |
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US7605469B2 (en) * | 2004-06-30 | 2009-10-20 | Intel Corporation | Atomic layer deposited tantalum containing adhesion layer |
JP2009016782A (ja) * | 2007-06-04 | 2009-01-22 | Tokyo Electron Ltd | 成膜方法及び成膜装置 |
TWI382987B (zh) * | 2007-07-24 | 2013-01-21 | Sigma Aldrich Co | 應用於化學相沉積製程的有機金屬前驅物 |
TWI425110B (zh) | 2007-07-24 | 2014-02-01 | Sigma Aldrich Co | 以化學相沉積法製造含金屬薄膜之方法 |
CN102112654B (zh) * | 2008-08-01 | 2013-03-20 | 乔治洛德方法研究和开发液化空气有限公司 | 在基质上形成含钽层的方法 |
DE102011078928A1 (de) | 2011-07-11 | 2013-01-17 | Carl Zeiss Smt Gmbh | Beleuchtungsoptik für die Projektionslithografie |
KR102627456B1 (ko) * | 2015-12-21 | 2024-01-19 | 삼성전자주식회사 | 탄탈럼 화합물과 이를 이용한 박막 형성 방법 및 집적회로 소자의 제조 방법 |
TW201741490A (zh) * | 2016-05-27 | 2017-12-01 | Tes股份有限公司 | 金屬碳膜的沈積方法 |
JP6777933B2 (ja) * | 2016-12-02 | 2020-10-28 | 株式会社高純度化学研究所 | 化学蒸着用原料及びその製造方法、並びに該化学蒸着用原料を用いて形成されるインジウムを含有する酸化物の膜の製造方法 |
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US5130172A (en) * | 1988-10-21 | 1992-07-14 | The Regents Of The University Of California | Low temperature organometallic deposition of metals |
US6015917A (en) * | 1998-01-23 | 2000-01-18 | Advanced Technology Materials, Inc. | Tantalum amide precursors for deposition of tantalum nitride on a substrate |
US6491987B2 (en) * | 1999-05-03 | 2002-12-10 | Guardian Indusries Corp. | Process for depositing DLC inclusive coating with surface roughness on substrate |
US6743473B1 (en) * | 2000-02-16 | 2004-06-01 | Applied Materials, Inc. | Chemical vapor deposition of barriers from novel precursors |
US6989457B2 (en) * | 2003-01-16 | 2006-01-24 | Advanced Technology Materials, Inc. | Chemical vapor deposition precursors for deposition of tantalum-based materials |
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JP5053543B2 (ja) | 2012-10-17 |
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WO2006082739A1 (ja) | 2006-08-10 |
KR20070101352A (ko) | 2007-10-16 |
JP2007084522A (ja) | 2007-04-05 |
EP1852438A1 (de) | 2007-11-07 |
TW200635939A (en) | 2006-10-16 |
EP1852438A4 (de) | 2008-02-06 |
US20090043119A1 (en) | 2009-02-12 |
CN101111502A (zh) | 2008-01-23 |
US7592471B2 (en) | 2009-09-22 |
TWI369360B (en) | 2012-08-01 |
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